Your browser doesn't support javascript.
loading
COMTVal158Met polymorphism is associated with ecstasy (MDMA)-induced psychotic symptoms in the Turkish population.
Aytac, Hasan Mervan; Oyaci, Yasemin; Aydin, Pinar Cetinay; Pehlivan, Mustafa; Pehlivan, Sacide.
Afiliación
  • Aytac HM; From the Department of Psychiatry (Aytac), Basaksehir Cam and Sakura City Hospital; Department of Medical Biology (Oyaci, Pehlivan), Istanbul Faculty of Medicine, Istanbul University, and from the Department of Psychiatry (Cetinay Aydin), Bakirkoy Research and Training Hospital for Psychiatry, Neuro
  • Oyaci Y; From the Department of Psychiatry (Aytac), Basaksehir Cam and Sakura City Hospital; Department of Medical Biology (Oyaci, Pehlivan), Istanbul Faculty of Medicine, Istanbul University, and from the Department of Psychiatry (Cetinay Aydin), Bakirkoy Research and Training Hospital for Psychiatry, Neuro
  • Aydin PC; From the Department of Psychiatry (Aytac), Basaksehir Cam and Sakura City Hospital; Department of Medical Biology (Oyaci, Pehlivan), Istanbul Faculty of Medicine, Istanbul University, and from the Department of Psychiatry (Cetinay Aydin), Bakirkoy Research and Training Hospital for Psychiatry, Neuro
  • Pehlivan M; From the Department of Psychiatry (Aytac), Basaksehir Cam and Sakura City Hospital; Department of Medical Biology (Oyaci, Pehlivan), Istanbul Faculty of Medicine, Istanbul University, and from the Department of Psychiatry (Cetinay Aydin), Bakirkoy Research and Training Hospital for Psychiatry, Neuro
  • Pehlivan S; From the Department of Psychiatry (Aytac), Basaksehir Cam and Sakura City Hospital; Department of Medical Biology (Oyaci, Pehlivan), Istanbul Faculty of Medicine, Istanbul University, and from the Department of Psychiatry (Cetinay Aydin), Bakirkoy Research and Training Hospital for Psychiatry, Neuro
Neurosciences (Riyadh) ; 27(1): 24-30, 2022 Jan.
Article en En | MEDLINE | ID: mdl-35017287
ABSTRACT

OBJECTIVES:

To investigate catechol-O-methyltransferase (COMT) Val158Met gene polymorphism in MDMA use disorder (MUD) by comparing genotype distributions between MUD patients and healthy controls considering clinical parameters.

METHODS:

Eighty-two MUD patients' were consecutively admitted to the outpatient psychiatry clinic in May 2019-January 2020, and 95 healthy volunteers were included in the case-control study. We used the polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) to determine COMT Val158Met polymorphism.

RESULTS:

The COMT Val158Met genotype distribution and allele frequencies of the MUD patient group were significantly different from the healthy control group. The Met/Met genotype (OR 2.692; 95% Cl 1.272-5.698; p=0.008) and Met allele frequencies (OR 1.716; 95% Cl 1.118-2.633; p=0.013) were significantly higher in the control group than in MUD patients. When the COMT Val158Met genotype and allele frequency distributions were compared between 2 groups according to the psychotic symptoms in the MUD patient group, the COMT Val158Met genotype distributions were significantly different between the groups of patients. The percentage of patients with the Val/Val genotype was significantly lower in MUD patients with a psychotic symptom than the MUD patients without a psychotic symptom (OR 2.625; 95% Cl 1.069-6.446; p=0.033).

CONCLUSION:

The COMT Val158Met gene polymorphism was found to be related to the MUD-diagnosed Turkish patients and MDMA-induced psychotic symptoms.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Psicosis Inducidas por Sustancias / Catecol O-Metiltransferasa / N-Metil-3,4-metilenodioxianfetamina Tipo de estudio: Diagnostic_studies / Observational_studies / Risk_factors_studies País/Región como asunto: Asia Idioma: En Revista: Neurosciences (Riyadh) Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Psicosis Inducidas por Sustancias / Catecol O-Metiltransferasa / N-Metil-3,4-metilenodioxianfetamina Tipo de estudio: Diagnostic_studies / Observational_studies / Risk_factors_studies País/Región como asunto: Asia Idioma: En Revista: Neurosciences (Riyadh) Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article